Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58109641T>ACA353343472FLNBn.2408T>A
c.2265T>A (p.Ser755Arg)
c.*797T>A (n.*797T>A)
c.1758T>A (p.Ser586Arg)
n.2410T>A
3g.58109641T>CCA434033741FLNBn.2408T>C
c.2265T>C (p.Ser755=)
c.*797T>C (n.*797T>C)
c.1758T>C (p.Ser586=)
n.2410T>C
3g.58109641T>GCA353343475FLNBn.2408T>G
c.2265T>G (p.Ser755Arg)
c.*797T>G (n.*797T>G)
c.1758T>G (p.Ser586Arg)
n.2410T>G
3g.58109642G>ACA353343478FLNBn.2409G>A
c.2266G>A (p.Gly756Ser)
c.*798G>A (n.*798G>A)
c.1759G>A (p.Gly587Ser)
n.2411G>A
3g.58109642G>CCA353343479FLNBn.2409G>C
c.2266G>C (p.Gly756Arg)
c.*798G>C (n.*798G>C)
c.1759G>C (p.Gly587Arg)
n.2411G>C
3g.58109642G>TCA353343482FLNBn.2409G>T
c.2266G>T (p.Gly756Cys)
c.*798G>T (n.*798G>T)
c.1759G>T (p.Gly587Cys)
n.2411G>T
COSMIC COSMIC
3g.58109643G>ACA353343487FLNBn.2410G>A
c.2267G>A (p.Gly756Asp)
c.*799G>A (n.*799G>A)
c.1760G>A (p.Gly587Asp)
n.2412G>A
dbSNP COSMIC COSMIC COSMIC
3g.58109643G>CCA353343489FLNBn.2410G>C
c.2267G>C (p.Gly756Ala)
c.*799G>C (n.*799G>C)
c.1760G>C (p.Gly587Ala)
n.2412G>C
COSMIC COSMIC
3g.58109643G=CA1367500647FLNBn.2410G=
c.2267G= (p.Gly756=)
c.*799G= (n.*799G=)
c.1760G= (p.Gly587=)
n.2412G=
3g.58109643G>TCA353343485FLNBn.2410G>T
c.2267G>T (p.Gly756Val)
c.*799G>T (n.*799G>T)
c.1760G>T (p.Gly587Val)
n.2412G>T
3g.58109644T>ACA434033760FLNBn.2411T>A
c.2268T>A (p.Gly756=)
c.*800T>A (n.*800T>A)
c.1761T>A (p.Gly587=)
n.2413T>A
dbSNP gnomAD v2 gnomAD v4
3g.58109644T>CCA434033762FLNBn.2411T>C
c.2268T>C (p.Gly756=)
c.*800T>C (n.*800T>C)
c.1761T>C (p.Gly587=)
n.2413T>C
3g.58109644T>GCA434033767FLNBn.2411T>G
c.2268T>G (p.Gly756=)
c.*800T>G (n.*800T>G)
c.1761T>G (p.Gly587=)
n.2413T>G
3g.58109644T=CA1367500648FLNBn.2411T=
c.2268T= (p.Gly756=)
c.*800T= (n.*800T=)
c.1761T= (p.Gly587=)
n.2413T=
3g.58109645C>ACA353343492FLNBn.2412C>A
c.2269C>A (p.Leu757Met)
c.*801C>A (n.*801C>A)
c.1762C>A (p.Leu588Met)
n.2414C>A
3g.58109645C>GCA353343494FLNBn.2412C>G
c.2269C>G (p.Leu757Val)
c.*801C>G (n.*801C>G)
c.1762C>G (p.Leu588Val)
n.2414C>G
3g.58109645C>TCA434033774FLNBn.2412C>T
c.2269C>T (p.Leu757=)
c.*801C>T (n.*801C>T)
c.1762C>T (p.Leu588=)
n.2414C>T
gnomAD v4
3g.58109646T>ACA353343497FLNBn.2413T>A
c.2270T>A (p.Leu757Gln)
c.*802T>A (n.*802T>A)
c.1763T>A (p.Leu588Gln)
n.2415T>A
3g.58109646T>CCA353343499FLNBn.2413T>C
c.2270T>C (p.Leu757Pro)
c.*802T>C (n.*802T>C)
c.1763T>C (p.Leu588Pro)
n.2415T>C
3g.58109646T>GCA353343501FLNBn.2413T>G
c.2270T>G (p.Leu757Arg)
c.*802T>G (n.*802T>G)
c.1763T>G (p.Leu588Arg)
n.2415T>G
3g.58109647G>ACA434033782FLNBn.2414G>A
c.2271G>A (p.Leu757=)
c.*803G>A (n.*803G>A)
c.1764G>A (p.Leu588=)
n.2416G>A
dbSNP gnomAD v4
3g.58109647G>CCA434033785FLNBn.2414G>C
c.2271G>C (p.Leu757=)
c.*803G>C (n.*803G>C)
c.1764G>C (p.Leu588=)
n.2416G>C
3g.58109647G=CA1367500649FLNBn.2414G=
c.2271G= (p.Leu757=)
c.*803G= (n.*803G=)
c.1764G= (p.Leu588=)
n.2416G=
3g.58109647G>TCA434033788FLNBn.2414G>T
c.2271G>T (p.Leu757=)
c.*803G>T (n.*803G>T)
c.1764G>T (p.Leu588=)
n.2416G>T
3g.58109648A>CCA353343502FLNBn.2415A>C
c.2272A>C (p.Lys758Gln)
c.*804A>C (n.*804A>C)
c.1765A>C (p.Lys589Gln)
n.2417A>C
3g.58109648A>GCA353343505FLNBn.2415A>G
c.2272A>G (p.Lys758Glu)
c.*804A>G (n.*804A>G)
c.1765A>G (p.Lys589Glu)
n.2417A>G
3g.58109648A>TCA353343507FLNBn.2415A>T
c.2272A>T (p.Lys758Ter)
c.*804A>T (n.*804A>T)
c.1765A>T (p.Lys589Ter)
n.2417A>T
3g.58109649A>CCA353343510FLNBn.2416A>C
c.2273A>C (p.Lys758Thr)
c.*805A>C (n.*805A>C)
c.1766A>C (p.Lys589Thr)
n.2418A>C
3g.58109649A>GCA353343513FLNBn.2416A>G
c.2273A>G (p.Lys758Arg)
c.*805A>G (n.*805A>G)
c.1766A>G (p.Lys589Arg)
n.2418A>G
3g.58109649A>TCA353343515FLNBn.2416A>T
c.2273A>T (p.Lys758Met)
c.*805A>T (n.*805A>T)
c.1766A>T (p.Lys589Met)
n.2418A>T
3g.58109650G>ACA434033801FLNBn.2417G>A
c.2274G>A (p.Lys758=)
c.*806G>A (n.*806G>A)
c.1767G>A (p.Lys589=)
n.2419G>A
3g.58109650G>CCA353343517FLNBn.2417G>C
c.2274G>C (p.Lys758Asn)
c.*806G>C (n.*806G>C)
c.1767G>C (p.Lys589Asn)
n.2419G>C
3g.58109650G>TCA353343519FLNBn.2417G>T
c.2274G>T (p.Lys758Asn)
c.*806G>T (n.*806G>T)
c.1767G>T (p.Lys589Asn)
n.2419G>T
3g.58109651G>ACA2468064FLNBn.2418G>A
c.2275G>A (p.Ala759Thr)
c.*807G>A (n.*807G>A)
c.1768G>A (p.Ala590Thr)
n.2420G>A
dbSNP ExAC gnomAD v2 gnomAD v4
3g.58109651G>CCA353343525FLNBn.2418G>C
c.2275G>C (p.Ala759Pro)
c.*807G>C (n.*807G>C)
c.1768G>C (p.Ala590Pro)
n.2420G>C
3g.58109651G=CA1367500650FLNBn.2418G=
c.2275G= (p.Ala759=)
c.*807G= (n.*807G=)
c.1768G= (p.Ala590=)
n.2420G=
3g.58109651G>TCA353343522FLNBn.2418G>T
c.2275G>T (p.Ala759Ser)
c.*807G>T (n.*807G>T)
c.1768G>T (p.Ala590Ser)
n.2420G>T
3g.58109652C>ACA353343530FLNBn.2419C>A
c.2276C>A (p.Ala759Glu)
c.*808C>A (n.*808C>A)
c.1769C>A (p.Ala590Glu)
n.2421C>A
gnomAD v4
3g.58109652C>GCA353343532FLNBn.2419C>G
c.2276C>G (p.Ala759Gly)
c.*808C>G (n.*808C>G)
c.1769C>G (p.Ala590Gly)
n.2421C>G
3g.58109652C>TCA353343534FLNBn.2419C>T
c.2276C>T (p.Ala759Val)
c.*808C>T (n.*808C>T)
c.1769C>T (p.Ala590Val)
n.2421C>T
3g.58109653A>CCA434033816FLNBn.2420A>C
c.2277A>C (p.Ala759=)
c.*809A>C (n.*809A>C)
c.1770A>C (p.Ala590=)
n.2422A>C
3g.58109653A>GCA434033817FLNBn.2420A>G
c.2277A>G (p.Ala759=)
c.*809A>G (n.*809A>G)
c.1770A>G (p.Ala590=)
n.2422A>G
gnomAD v4
3g.58109653A>TCA434033819FLNBn.2420A>T
c.2277A>T (p.Ala759=)
c.*809A>T (n.*809A>T)
c.1770A>T (p.Ala590=)
n.2422A>T
3g.58109654A=CA1367500651FLNBn.2421A=
c.2278A= (p.Asn760=)
c.*810A= (n.*810A=)
c.1771A= (p.Asn591=)
n.2423A=
3g.58109654A>CCA353343537FLNBn.2421A>C
c.2278A>C (p.Asn760His)
c.*810A>C (n.*810A>C)
c.1771A>C (p.Asn591His)
n.2423A>C
3g.58109654A>GCA353343539FLNBn.2421A>G
c.2278A>G (p.Asn760Asp)
c.*810A>G (n.*810A>G)
c.1771A>G (p.Asn591Asp)
n.2423A>G
dbSNP gnomAD v3 gnomAD v4
3g.58109654A>TCA353343541FLNBn.2421A>T
c.2278A>T (p.Asn760Tyr)
c.*810A>T (n.*810A>T)
c.1771A>T (p.Asn591Tyr)
n.2423A>T
3g.58109655A>CCA353343544FLNBn.2422A>C
c.2279A>C (p.Asn760Thr)
c.*811A>C (n.*811A>C)
c.1772A>C (p.Asn591Thr)
n.2424A>C
3g.58109655A>GCA353343546FLNBn.2422A>G
c.2279A>G (p.Asn760Ser)
c.*811A>G (n.*811A>G)
c.1772A>G (p.Asn591Ser)
n.2424A>G
COSMIC COSMIC COSMIC
3g.58109655A>TCA353343548FLNBn.2422A>T
c.2279A>T (p.Asn760Ile)
c.*811A>T (n.*811A>T)
c.1772A>T (p.Asn591Ile)
n.2424A>T
gnomAD v4

Number of alleles fetched